Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Q-CLEAR

K-Number: K110370 · 2011-09-15

ApplicantLight Age, Inc.
Decision Date2011-09-15
Product CodePDZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Q-CLEAR is the device name listed in this FDA 510(k) record. The listed applicant is Light Age, Inc.. It received FDA 510(k) clearance on 2011-09-15 under 510(k) number K110370. The device is classified under product code PDZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q-CLEAR?

Q-CLEAR is a medical device that received FDA 510(k) clearance on 2011-09-15. The listed applicant is Light Age, Inc.. The 510(k) number is K110370.

When did Q-CLEAR receive FDA 510(k) clearance?

Q-CLEAR received FDA 510(k) clearance on 2011-09-15, under 510(k) number K110370.

Who is the listed applicant for Q-CLEAR?

The FDA 510(k) record lists Light Age, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q-CLEAR?

The FDA product code for Q-CLEAR is PDZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Light Age, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113115EPICARE YAGK091625EPICARE-DUO LASER SYSTEMK032991LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPXK033259LIGHT AGE Q-CLEAR LASER, MODEL 701-1101K983977LIGHT AGE EPICARE ALEXANDRITE LASERK980131ALEX TA2 ERASER

View all 7 devices →

Related Devices (Code: PDZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253960Medicell Mycosis Laser (MCML24004)Medicell Healthcare Co.,LTDK241116Onycho Laser VTerasysd&C, Inc.K211265TFX-LT2000 Therapy LightToefx, Inc.K221363AF LaserShenB Co., Ltd.K190034REMY Medical Therapy Laser SystemFootdocprenur, LLCK153164LunulaLaserErchonia Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑